These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
127 related articles for article (PubMed ID: 14994281)
1. Preface: fragile X syndrome: frontiers of understanding gene-brain-behavior relationships. Crnic LS; Hagerman R Ment Retard Dev Disabil Res Rev; 2004; 10(1):1-2. PubMed ID: 14994281 [No Abstract] [Full Text] [Related]
2. Fragile X syndrome: a model of gene-brain-behavior relationships. Hagerman RJ; Hagerman PJ Mol Genet Metab; 2001; 74(1-2):89-97. PubMed ID: 11592806 [No Abstract] [Full Text] [Related]
3. [Fragile X syndrome: a model of gene-brain-behaviour relationships]. Hagerman RJ; Hagerman PJ Rev Neurol; 2001 Oct; 33 Suppl 1():S51-7. PubMed ID: 12447820 [TBL] [Abstract][Full Text] [Related]
4. [Mental retardation and fragile X syndrome]. Nanba E No To Shinkei; 1998 Apr; 50(4):317-23. PubMed ID: 9592820 [No Abstract] [Full Text] [Related]
5. Neurobiology of Fragile X syndrome: from molecular genetics to neurobehavioral phenotype. Kaufmann WE Microsc Res Tech; 2002 May; 57(3):131-4. PubMed ID: 12112447 [No Abstract] [Full Text] [Related]
6. Fragile X syndrome. Terracciano A; Chiurazzi P; Neri G Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):32-7. PubMed ID: 16010677 [TBL] [Abstract][Full Text] [Related]
7. A new regulatory pathway for fragile X syndrome? Hansen RS; Laird CD Nat Med; 2002 Nov; 8(11):1204-5. PubMed ID: 12411943 [No Abstract] [Full Text] [Related]
8. The fragile-X syndrome after the discovery of the FMR-1 gene. The clinical geneticist faced with the unravelled enigmas and persisting difficulties in genetic counseling. Fryns JP; Curfs LM; Cassiman JJ; van den Berghe H Genet Couns; 1992; 3(4):175-7. PubMed ID: 1361752 [No Abstract] [Full Text] [Related]
9. Translational complexity of the fragile x mental retardation protein: insights from the fly. Broadie K; Pan L Mol Cell; 2005 Mar; 17(6):757-9. PubMed ID: 15780932 [TBL] [Abstract][Full Text] [Related]
10. Molecular diagnosis and genetic counseling for fragile X mental retardation. Pandey UB; Phadke SR; Mittal B Neurol India; 2004 Mar; 52(1):36-42. PubMed ID: 15069237 [TBL] [Abstract][Full Text] [Related]
11. Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene. Fryns JP; D'Hooghe M; Devriendt K Genet Couns; 1996; 7(3):227-30. PubMed ID: 8897045 [TBL] [Abstract][Full Text] [Related]
12. [Fragile X syndrome, a disease caused by defects in an RNA-binding protein]. Siomi MC; Siomi H Tanpakushitsu Kakusan Koso; 2003 Mar; 48(4 Suppl):480-6. PubMed ID: 12696157 [No Abstract] [Full Text] [Related]
13. The fragile X syndrome: from molecular genetics to neurobiology. Willemsen R; Oostra BA; Bassell GJ; Dictenberg J Ment Retard Dev Disabil Res Rev; 2004; 10(1):60-7. PubMed ID: 14994290 [TBL] [Abstract][Full Text] [Related]
14. Understanding Fragile X syndrome: molecular, cellular and genomic neuroscience at the crossroads. Moldin SO Genes Brain Behav; 2005 Aug; 4(6):337-40. PubMed ID: 16098132 [No Abstract] [Full Text] [Related]
15. Molecular screening for fragile X syndrome among Indonesian children with developmental disability. Faradz SM; Buckley M; Lam-Po-Tang ; Leigh D; Holden JJ Am J Med Genet; 1999 Apr; 83(4):350-1. PubMed ID: 10208179 [No Abstract] [Full Text] [Related]
16. Fragile X mental retardation syndrome: from pathogenesis to diagnostic issues. Mandel JL; Biancalana V Growth Horm IGF Res; 2004 Jun; 14 Suppl A():S158-65. PubMed ID: 15135801 [TBL] [Abstract][Full Text] [Related]
17. Dilemmas in counselling females with the fragile X syndrome. de Vries BB; van den Boer-van den Berg HM; Niermeijer MF; Tibben A J Med Genet; 1999 Feb; 36(2):167-70. PubMed ID: 10051021 [TBL] [Abstract][Full Text] [Related]
18. Biomedicine. Do G quartets orchestrate fragile X pathology? Moine H; Mandel JL Science; 2001 Dec; 294(5551):2487-8. PubMed ID: 11752559 [No Abstract] [Full Text] [Related]
19. DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature. Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; Morel ML; Rousseau F Am J Med Genet; 1999 Apr; 83(4):347-9. PubMed ID: 10208178 [No Abstract] [Full Text] [Related]
20. [Discovery of the gene defect in fragile X syndrome reveals a new mode of inheritance and improves diagnosis]. von Koskull H; Leisti J Duodecim; 1992; 108(17):1445-7. PubMed ID: 1366164 [No Abstract] [Full Text] [Related] [Next] [New Search]